Multilocus association mapping using variable-length markov chainsBROWNING, Sharon R.American journal of human genetics. 2006, Vol 78, Num 6, pp 903-913, issn 0002-9297, 11 p.Article

Missing data imputation and haplotype phase inference for genome-wide association studiesBROWNING, Sharon R.Human genetics. 2008, Vol 124, Num 5, pp 439-450, issn 0340-6717, 12 p.Article

A Fast, Powerful Method for Detecting Identity by DescentBROWNING, Brian L; BROWNING, Sharon R.American journal of human genetics. 2011, Vol 88, Num 2, pp 173-182, issn 0002-9297, 10 p.Article

High-Resolution Detection of Identity by Descent in Unrelated IndividualsBROWNING, Sharon R; BROWNING, Brian L.American journal of human genetics. 2010, Vol 86, Num 4, pp 526-539, issn 0002-9297, 14 p.Article

A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated IndividualsBROWNING, Brian L; BROWNING, Sharon R.American journal of human genetics. 2009, Vol 84, Num 2, pp 210-223, issn 0002-9297, 14 p.Article

Haplotype phasing: existing methods and new developmentsBROWNING, Sharon R; BROWNING, Brian L.Nature reviews. Genetics (Print). 2011, Vol 12, Num 10, pp 703-714, issn 1471-0056, 12 p.Article

Haplotypic analysis of Wellcome Trust Case Control Consortium dataBROWNING, Brian L; BROWNING, Sharon R.Human genetics. 2008, Vol 123, Num 3, pp 273-280, issn 0340-6717, 8 p.Article

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clusteringBROWNING, Sharon R; BROWNING, Brian L.American journal of human genetics. 2007, Vol 81, Num 5, pp 1084-1097, issn 0002-9297, 14 p.Article

A Canine Model of Inherited Myopia : Familial Aggregation of Refractive Error in Labrador RetrieversBLACK, Joanna; BROWNING, Sharon R; COLLINS, Andrew V et al.Investigative ophthalmology & visual science. 2008, Vol 49, Num 11, pp 4784-4789, issn 0146-0404, 6 p.Article

Case-control single-marker and haplotypic association analysis of pedigree dataBROWNING, Sharon R; BRILEY, J. David; WAGNER, Michael J et al.Genetic epidemiology. 2005, Vol 28, Num 2, pp 110-122, issn 0741-0395, 13 p.Article

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delayGIRIRAJAN, Santhosh; ROSENFELD, Jill A; MEFFORD, Heather C et al.Nature genetics. 2010, Vol 42, Num 3, pp 203-209, issn 1061-4036, 7 p.Article

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray StudiesBAHLO, Melanie; STANKOVICH, Jim; DANOY, Patrick et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 3, pp 794-798, issn 1055-9965, 5 p.Article